Huntleigh Smartsigns Compact SC750 User manual

1
Table of Contents
TABLE OF CONTENTS
1. Warnings .................................................................... 2
1.1 Cautions .............................................................................. 2
2. INTRODUCTION .......................................................... 4
2.1 Contents.............................................................................. 4
2.2 Front Panel .......................................................................... 8
2.3 Rear Panel ........................................................................... 9
2.4 Switching On ....................................................................... 10
2.5 Switching Off....................................................................... 10
3. Operation.................................................................... 11
3.1 Application Screen .............................................................. 11
3.2 Command Bar ..................................................................... 12
3.2.1 Setup............................................................................................ 12
4. Patient Monitoring...................................................... 14
4.1 ECG Monitoring ................................................................... 14
4.2 Respiration Monitoring........................................................ 15
4.3 SpO2 Monitoring ................................................................. 16
4.4 Temperature Monitoring ...................................................... 17
4.5 NIBP Monitoring .................................................................. 18
5. Recorder Setup .......................................................... 19
6. Technical Data............................................................ 20
7. Care of your Equipment ............................................. 23
7.1 Cleaning and Disinfecting................................................... 23
8. Warranty & Service..................................................... 25
HEALTHCARE

2
1. Warnings
Before using this equipment, please study this manual
carefully and familiarise yourself with the controls, display
features and operating techniques. Ensure each user fully
understands the safety and operation of the unit, as mis-use
may cause damage to the unit or injury to the user or the
patient.
This equipment has been manufactured using quality components
and designed to operate safely and reliably.
If the integrity of the protective earth conductor is in doubt, the
equipment should be operated from its internal electrical power
source.
All modifications and repairs to the equipment must carried out
by qualified service engineers, agents or hospital technicians
authorised by Huntleigh Healthcare.
CE MARKING
This equipment carries a CE mark but this is only fully valid if it is used
in conjunction with cables and other accessories approved by Huntleigh
Healthcare Ltd.
1.1 Cautions
Note The following are descriptions of general hazards and unsafe
practices that could result in death, severe injury or product
damage. Specific warnings and cautions not appearing in
this section are found throughout the manual.
Possible Fire or
Explosion
A possible explosion hazard exists if used in the presence of
flammable anaesthetics. Explosion or fire can result.
Possible Safety
Hazard
Do not mount the equipment directly above the patient.
Place the equipment in a location where it cannot harm the
patient should it fall from its shelf or other mount.
Possible
Electrical Hazard
Do not operate the equipment using damaged cables and
wires, or loose snap fittings, which may cause interference
or loss of signal.
Perform frequent electrical and visual inspections on cables
and wires.
Possible Shock
or Fire Hazard
Do not immerse any portion of the instrument in water. Fluid
spills may damage the instrument’s electrical components.
Warnings

3
Possible
Equipment
Damage
Do not sterilise this product. Sterilisation environments can
cause severe damage.
Do not autoclave or gas sterilise accessories unless
manufacturer instructions clearly approve it.
Possible Safety
Risk
Do not substitute accessories. Use only recommended
accessories listed in this manual. Substitution may cause
the instrument to work improperly. The correct accessories
are shielded to prevent conductive parts of the electrodes
contacting other conductive parts or earth. No action should
be taken which permits this to happen.
Warning All interconnecting equipment must meet their relevant
safety standards i.e. EN60959 in the case of computers,
network terminals and display monitors. When several
pieces of equipment of various origins are interconnected,
the summation of leakage currents may constitute a hazard.
Warning The accuracy of the readings obtained from this equipment
may be affected by the presence of a pacemaker or by
cardiac arrhythmia
Warning If it is thought that interference is occurring from or with
other equipment, such as that used for Diathermy, then
either shut-off, or move, the offending devices, increase the
separation or reduce lead lengths.
Warning If the integrity of the protective earth conductor arrangement
is in doubt, the equipment should be operated from its
internal electrical power source only while connected to a
patient. Use the mains supply only to re-charge the battery
while not connected to a patient
Caution Electromagnetic Compatibility (EMC). This product complies
with the requirements of applicable EMC Standards. The use
of accessories not specified by the manufacturer may result
in increased emissions by, or decreased immunity of, the
equipment, affecting its performance.
This product contains sensitive electronics; strong radio
frequency fields could interfere with the operation of the
system. In the event where this occurs, we suggest that the
source of interference is identified and the equipment is used
‘out of range’.
Do not use this equipment in the presence of flammable gases.
Do not immerse any part of the equipment in any liquids.
Do not use solvent cleaner on any part of the system.
Do not use high temperature sterilising or E-beam / gamma sterilisation
processes.
If any doubt exists concerning the use of this equipment, an
alternative method should be used.
Warnings

4
2. Introduction
2.1 Contents
CHG
HEALTHCARE
SC750SC750
1 X SC750
1 X Mains Lead
1 X User Manual
Introduction

5
1 X Adult Finger Sensor
1 X SpO2 Interface Cable
1 X ECG/RESP Patient Cable
Temperature Probes (optional)
1 X Surface
1 X Rectal
1 X Central
ECG / RESP
Introduction

6
1 X NIBP Hose
1 X Standard Adult Cuff
NIBP
Recorder
1 X Chart Paper
Introduction

7
Loading Chart Paper
1.
2.
4.
10cm
3.
1. Open the door.
2. Insert / Replace chart paper
3. Align paper to roller.
4. Close the door
Introduction

8
2.2 Front Panel
CHG
HEALTHCARE
SC750SC750
1~Green “~ “ ON Indicates mains power connected.
2CHG Yellow “CHG” ON Indicates that the internal battery is charging.
3Yellow above the “On” / Off” button indicates the unit is switched
on.
Introduction

9
2.3 Rear Panel
1External DC Input
2Mains Input Socket
3Mains ON/OFF Switch
4
I/O Sockets (from the top) :
• Ethernet Socket
• Serial Port
• Keyboard Socket
• External Monitor Socket
• Equipotential Earth Connector
5Integral Battery Access Cover
6Rating and Serial Number Label
1
2
3
4
5
6
Introduction

10
2.3 Switching On
1. Connect the SC750 to
mains outlet as shown
Use only with a 250V fuse
Employer uniquement avec
un fusible de 250V
Use only with a 250V fuse
Employer uniquement avec
un fusible de 250V
o
I
2.
1.
2. Switch On
3.
3. LED will illuminate
4.
4. Press . .
CHANGE DETAILS
CONTINUE
SC750
NAME: SOMEBODY
REF: ABC-01234-DE
BED NUMBER: 2
HEALTHCARE
5.
5. Opening Screen will be
displayed.
2.4 Switching Off
1. Press . .
Press CHANGE DETAILS or CONTINUE.
Yes
No
Shut Down?
Introduction

11
3.1 Application Screen
3. Operation
The screen is arranged into a series of waveforms and numercal indicators.
15
br/m
18 : 05
85%
40.0
50
11
°C
30.0
40.0
30.0
T1
T2
37.9
38.1
0.2
60
mmHg
AUTO 5
11 Apr 2005
160
50
MAP
DIA
SYS
SETUP SUSPEND TRENDS SPOT RECORD
GO/STOP
N
I
B
P
REC : OK (MANUAL)
ADULT
SOMEBODY
PATIENT REF
I
N
F
O
T
E
M
P
1 /cm
R
E
S
P
97
%bpm
100
92
90
30
S
P
O
2
HEALTHCARE
Lead i (CASC)
E
C
G
60
Lead I bpm
x1
90
30
E
C
G
18 : 05
85%
11 Apr 2005
HEALTHCARE
REC : OK (MANUAL)
ADULT
SOMEBODY
PATIENT REF
I
N
F
O
Patients name
and number
Date, time and
battery status
Touchscreen
lock / Unlock
Command Bar
Parameter Identification
Operation

12
3.2 Command Bar
Press any of the command bar TABS to view or change settings:-
3.2.1 Setup
SETUP
SETUP
SYSTEM
PATIENT
ECG
RECORDER
RESP
SPO2TEMP
NIBP
TRENDS
25mm/s
ALARM SETUP
Speed
6.25mm/s
12.5mm/s
50mm/s
SEE
SECTION 4
SETUP SUSPEND TRENDS SPOT RECORD
GO/STOP
System
Patient
Recorder
Monitroring Capability
Trends
Alarm Setup
Suspend
Alarm
TRENDS Set
up Tabular/
Graphical
FREEZE/
Unfreeze
Trace
START/STOP
Recorder (If
fitted)
Operation
NUMERIC
Mode
1
2
3
4
5

13
SYSTEM
Brilliance
Volume
Volume
ENGLISH
SET TIME/DATE
Lang
2 MINUTES
Suspend
+- +- +-
DEMO MODE
SYSTEM SETUP FRANÇAIS
DEUTSCH
ESPAÑOL
PORTUGUÊS
SVENSKA
5 MINUTES
15 MINUTES
Time 16
8
26
Jan
2003
+- +-
Date
+- +- +-
hour
year
month
day
minute
TIME/DATE
1
PATIENT
PATIENT
Change Name/Ref
ADULT
New Patient?
Name
Ref
2
+-
Bed
NAME/REF
Name
Ref
A B C D E F
G H I J K L
M N O P Q R
S T U V W X
Y Z 0 1 2 3
4 5 6 7 8 9
DEL SPC
- . ' /
Mode
2
RECORDER
TRENDS
ALARM SETUP
TRENDS SETUP
Clear Trends
HR BR
%O
2
PR
T1 T2
Clear Trends
Confirm Clear
ALARM SETUP
OFF
HOLD ECG ALARMS
MEDIUM
(SOUND 1)
ECG ASYSTOLE
MEDIUM
(SOUND 1)
ECG HR low
MEDIUM
(SOUND 1)
ECG HR high
MEDIUM
(SOUND 1)
RESP APNOEA
MEDIUM
(SOUND 1)
RESP BR
high/low
ON
MEDIUM
(SOUND 2)
HIGH
(SOUND 1)
HIGH
(SOUND 2)
MEDIUM
(SOUND 2)
HIGH
(SOUND 1)
HIGH
(SOUND 2)
RECORDER SETUP
OFF
Wave 1
OFF
Wave 2
OFF
Wave 3
OFF
Wave 4
ON
Alarm Mode
RESET
OFF
ECG
RESP
SPO2
Operation

14
3.2.2 SPOT Mode
Press .
The screen will enter SPOT mode. All monitor functions, except ‘Freeze trace’
are active in SPOT mode.
18 : 05
85%
11 Apr 2005
SUSPEND TRENDS SPOT RECORD
GO/STOP
HEALTHCARE
60 97
60
124
85
(102)
80
ADULT
MANUAL
Lead II
@
18.05
SETUP
E
C
G
S
P
O
2
37.9
38.1
N
I
B
P
T
1
/
T
2
SPOT Mode
When the SPOT button is pressed on the command bar, the screen will
change to display ECG/SPO2/NIBP/TEMP in a large format.
Please note that no traces are displayed in SPOT mode.
SPOT
Press to return to normal mode.
SPOT
Operation

15
4.1 ECG Monitoring
1. Apply elecrodes to patient.
4. Patent Monitoring
2. Press . . .
3 LEAD
RA LA
LL
RA LA
LLRL
V1
5 LEAD
ECG SETUP
Lead
Gain
Mode
Filter
QRS Beep
OFF
MONITOR
x1
1mV
DUAL
ON
HR ALARM SETUP
OFF
x2, x4, x
12
DIAGNOSTIC
OFF
I
ON
ON
HR ALARM SETUP
Set Defaults
+
-
low
Use Defaults
Auto Limit
45
30
45 120
90
+
-
119
high
HR ALARM DEFAULTS
+
-
low
FACTORY DEFAULTS
46
45 120
+
-
119
high
I, II, III,
*aVR, aVL, aVF, V ON
Parameter
OFF
SETUP
3. Change as required.
4. Press √to save any changes.
ECG
Lead i (CASC)
E
C
G
60
Lead I bpm
x1
90
30
E
C
G
OR
* 5 Lead ECG option
Patient Monitoring

16
4.2 Respiration Monitoring
Respiration is detected via the ECG electrodes. In some situations it may be
necessary to reposition the electrodes as shown.
2. Press . . .
3 LEAD
RA LA
LL
RA LA
LLRL
V1
5 LEAD
ON
1 /cm
Parameter
RESP SETUP
Sens
BR ALARM SETUP
BR ALARM SETUP
Set Defaults
+
-
low
Use Defaults
Auto Limit
6
5
540
25
+
-
39
high
BR ALARM DEFAULTS
+
-
low
FACTORY DEFAULTS
5
540
+
-
40
high
OFF
SETUP
3. Change as required.
4. Press √to save any changes.
RESP 15
br/m
50
11
1 /cm
R
E
S
P
OR
Patient Monitoring

17
Patient Monitoring
4.3 SpO2 Monitoring
1. Apply sensor.
3. Press . . .
SPO 2 SETUP
ON
Parameter
Pulse Beep
ON
O2ALARM SETUP
PR ALARM SETUP
PR ALARM SETUP
Set Defaults
+
-
low
Use Defaults
Auto Limit
46
30
45 120
90
+
-
119
high
PR ALARM DEFAULTS
+
-
low
FACTORY DEFAULTS
45
45 120
+
-
120
high
OFF
O 2 ALARM SETUP
Set Defaults
+
-
low
Use Defaults
Auto Limit
93
95
92 100
99
+
-
99
high
O 2 ALARM DEFAULTS
+
-
low
FACTORY DEFAULTS
92
92 100
+
-
100
high
SETUP
4. Change as required.
5. Press √to save any changes.
SPO 2
60
97
%bpm
100
92
90
30
S
P
O
2
OR
2. Fix cable.

18
4.4 Temperature Monitoring
The system accepts a range of YSI 400 compatible temperature sensors.
These can be used for surface, central, oesophageal, nasopharyngeal and
rectal measurements.
1. Press . . .
TEMP SETUP
Parameter
T2 ALARM SETUP
T1 ALARM SETUP
T2 ALARM SETUP
Set Defaults
+
-
low
Use Defaults
Auto Limit
26.0
+
-
35.0
high
36.1
26.0 35.0
40.1
T1 ALARM SETUP
Set Defaults
+
-
low
Use Defaults
Auto Limit
26.0
36.9
26.0 35.0
38.9
+
-
35.0
high
T2 ALARM DEFAULTS
+
-
low
FACTORY DEFAULTS
26.0
+
-
35.0
high
35.5 39.5
T1 ALARM DEFAULTS
+
-
low
FACTORY DEFAULTS
26.0
35.5 39.5
+
-
35.0
high
SETUP
2. Change as required.
3. Press √to save any changes.
4. Follow the manufacturers user instructions for placement details.
TEMP
40.0
°C
30.0
40.0
30.0
T1
T2
37.9
38.1
0.2
T
E
M
P
OR
T1
T1
T2
T2
Single Channel Dual Channel
Patient Monitoring

19
Patient Monitoring
4.5 NIBP Monitoring
1. Apply Cuff to patient.
2. Press . . .
DIA ALARM SETUP
Set Defaults
+
-
low
Use Defaults
Auto Limit
41
60
40 100
100
+
-
99
high
DIA ALARM DEFAULTS
+
-
low
FACTORY DEFAULTS
40
40 100
+
-
100
high
MAP ALARM SETUP
Set Defaults
+
-
low
Use Defaults
Auto Limit
61
76
60 140
116
+
-
139
high
MAP ALARM DEFAULTS
+
-
low
FACTORY DEFAULTS
60
60 140
+
-
140
high
160 mmHg
AUTOMATIC
Start Pressure
5 Minutes
Cycle
DIA ALARM SETUP
MAP ALARM SETUP
SYS ALARM SETUP
ENABLE CALIBRATION MODE
NIBP SETUP
Mode
ADULT
Mode
NEONATAL
MANUAL
TURBO
160 mmHg
180 mmHg 100 mmHg
120 mmHg
Neonatal cuff mode
Adult cuff mode
2,3,4,5,10,15,30
60,90 minutes
SYS ALARM SETUP
Set Defaults
+
-
low
Use Defaults
Auto Limit
ON
81
100
80 160
140
+
-
159
high
SYS ALARM DEFAULTS
+
-
low
FACTORY DEFAULTS
80
80 160
+
-
160
high
OFF
SETUP
3. Change as required.
4. Press √to save any changes.
5. Press
NIBP
mmHg
AUTO 5 160
50
MAP
DIA
SYS
N
I
B
P
OR

20
RECORDER SETUP
OFF
Wave 1
OFF
Wave 2
OFF
Wave 3
OFF
Wave 4
ON
Alarm Mode
RESET
OFF
ECG
RESP
SPO2
1. Press . . .
5. Recorder Set-up
RECORDER
2. Change as required.
3. Press . . .
4. Press √to save any changes.
RESET
Alarm Mode
Alarm mode provides two options , ON or OFF.
Recorder will print automatically in the event of an alarm.
09 : 38 : 49 06 - Feb - 2002
NAME :
REF :
HR 60 bpm
BR 15 r / m
%02 97% PR 60 bpm
P1 :ART 120 / 80 (100) mmHg
P2 : CVP 15 . 0 / 9 . 6 ( 12 . 0 ) mmHg
CO2 40 mmHg RR 15 r / m
T1 37 .9 T2 38 .1
IBP1 SP02 RESP ECG
Position 1
Position 2
Position3
Position 4
ON
Press . . .
OFF
RECORD
GO/STOP
Recorder Setup